| 1i9y |
CRYSTAL STRUCTURE OF INOSITOL POLYPHOSPHATE 5-PHOSPHATASE DOMAIN (IPP5C) OF SPSYNAPTOJANIN |
23.9 |
91.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1i9z |
;CRYSTAL STRUCTURE OF INOSITOL POLYPHOSPHATE 5-PHOSPHATASE DOMAIN (IPP5C) OF SPSYNAPTOJANIN IN COMPLEX WITH INOSITOL (1,4)-BISPHOSPHATE AND CALCIUM ION
; |
24.1 |
92.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia0 |
KIF1A HEAD-MICROTUBULE COMPLEX STRUCTURE IN ATP-FORM |
33.8 |
115.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 1ia1 |
;Candida albicans dihydrofolate reductase complexed with dihydro-nicotinamide-adenine-dinucleotide phosphate (NADPH) and 5-(PHENYLSULFANYL)-2,4-QUINAZOLINEDIAMINE (GW997)
; |
25.6 |
82.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia2 |
;Candida albicans dihydrofolate reductase complexed with dihydro-nicotinamide-adenine-dinucleotide phosphate (NADPH) and 5-[(4-METHYLPHENYL)SULFANYL]-2,4-QUINAZOLINEDIAMINE (GW578)
; |
25.7 |
82.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia3 |
;Candida albicans dihydrofolate reductase complex in which the dihydronicotinamide moiety of dihydro-nicotinamide-adenine-dinucleotide phosphate (NADPH) is displaced by 5-[(4-TERT-BUTYLPHENYL)SULFANYL]-2,4-QUINAZOLINEDIAMINE (GW995)
; |
25.6 |
83.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia4 |
;Candida albicans dihydrofolate reductase complex in which the dihydronicotinamide moiety of dihydro-nicotinamide-adenine-dinucleotide phosphate (NADPH) is displaced by 5-{[4-(4-MORPHOLINYL)PHENYL]SULFANYL}-2,4-QUINAZOLINEDIAMIN (GW2021)
; |
25.6 |
82.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia5 |
POLYGALACTURONASE FROM ASPERGILLUS ACULEATUS |
21.8 |
70.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia6 |
CRYSTAL STRUCTURE OF THE CELLULASE CEL9M OF C. CELLULOLYTICUM |
21.3 |
65.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia7 |
CRYSTAL STRUCTURE OF THE CELLULASE CEL9M OF C. CELLULOLYTICIUM IN COMPLEX WITH CELLOBIOSE |
21.5 |
66.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia8 |
THE 1.7 A CRYSTAL STRUCTURE OF HUMAN CELL CYCLE CHECKPOINT KINASE CHK1 |
20.8 |
70.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1ia9 |
CRYSTAL STRUCTURE OF THE ATYPICAL PROTEIN KINASE DOMAIN OF A TRP CA-CHANNEL, CHAK (AMPPNP COMPLEX) |
33.8 |
115.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iaa |
;CRYSTAL STRUCTURES, SPECTROSCOPIC FEATURES, AND CATALYTIC PROPERTIES OF COBALT(II), COPPER(II), NICKEL(II), AND MERCURY(II) DERIVATIVES OF THE ZINC ENDOPEPTIDASE ASTACIN. A CORRELATION OF STRUCTURE AND PROTEOLYTIC ACTIVITY
; |
17.5 |
58.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iab |
;CRYSTAL STRUCTURES, SPECTROSCOPIC FEATURES, AND CATALYTIC PROPERTIES OF COBALT(II), COPPER(II), NICKEL(II), AND MERCURY(II) DERIVATIVES OF THE ZINC ENDOPEPTIDASE ASTACIN. A CORRELATION OF STRUCTURE AND PROTEOLYTIC ACTIVITY
; |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1iac |
;REFINED 1.8 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF ASTACIN, A ZINC-ENDOPEPTIDASE FROM THE CRAYFISH ASTACUS ASTACUS L. STRUCTURE DETERMINATION, REFINEMENT, MOLECULAR STRUCTURE AND COMPARISON WITH THERMOLYSIN
; |
17.4 |
56.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1iad |
;REFINED 1.8 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF ASTACIN, A ZINC-ENDOPEPTIDASE FROM THE CRAYFISH ASTACUS ASTACUS L. STRUCTURE DETERMINATION, REFINEMENT, MOLECULAR STRUCTURE AND COMPARISON TO THERMOLYSIN
; |
17.6 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1iae |
;CRYSTAL STRUCTURES, SPECTROSCOPIC FEATURES, AND CATALYTIC PROPERTIES OF COBALT(II), COPPER(II), NICKEL(II), AND MERCURY(II) DERIVATIVES OF THE ZINC ENDOPEPTIDASE ASTACIN. A CORRELATION OF STRUCTURE AND PROTEOLYTIC ACTIVITY
; |
17.5 |
56.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1iag |
FIRST STRUCTURE OF A SNAKE VENOM METALLOPROTEINASE: A PROTOTYPE FOR MATRIX METALLOPROTEINASES(SLASH)COLLAGENASES |
17.4 |
54.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1iah |
CRYSTAL STRUCTURE OF THE ATYPICAL PROTEIN KINASE DOMAIN OF A TRP CA-CHANNEL, CHAK (ADP-MG COMPLEX) |
33.7 |
111.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iai |
IDIOTYPE-ANTI-IDIOTYPE FAB COMPLEX |
39.5 |
139.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iaj |
CRYSTAL STRUCTURE OF THE ATYPICAL PROTEIN KINASE DOMAIN OF A TRP CA-CHANNEL, CHAK (APO) |
33.6 |
115.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iak |
HISTOCOMPATIBILITY ANTIGEN I-AK |
24.9 |
87.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ial |
IMPORTIN ALPHA, MOUSE |
28.3 |
98.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1iam |
STRUCTURE OF THE TWO AMINO-TERMINAL DOMAINS OF HUMAN INTERCELLULAR ADHESION MOLECULE-1, ICAM-1 |
24.5 |
90.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ian |
HUMAN P38 MAP KINASE INHIBITOR COMPLEX |
22.1 |
69.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1iao |
CLASS II MHC I-AD IN COMPLEX WITH OVALBUMIN PEPTIDE 323-339 |
24.4 |
81.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iap |
CRYSTAL STRUCTURE OF P115RHOGEF RGRGS DOMAIN |
18.6 |
63.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1iaq |
;C-H-RAS P21 PROTEIN MUTANT WITH THR 35 REPLACED BY SER (T35S) COMPLEXED WITH GUANOSINE-5'-[B,G-IMIDO] TRIPHOSPHATE
; |
25.3 |
80.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1iar |
INTERLEUKIN-4 / RECEPTOR ALPHA CHAIN COMPLEX |
24.2 |
81.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ias |
CYTOPLASMIC DOMAIN OF UNPHOSPHORYLATED TYPE I TGF-BETA RECEPTOR CRYSTALLIZED WITHOUT FKBP12 |
45.0 |
132.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iat |
CRYSTAL STRUCTURE OF HUMAN PHOSPHOGLUCOSE ISOMERASE/NEUROLEUKIN/AUTOCRINE MOTILITY FACTOR/MATURATION FACTOR |
27.2 |
86.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1iau |
HUMAN GRANZYME B IN COMPLEX WITH AC-IEPD-CHO |
18.3 |
61.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iav |
STRUCTURE ON NATIVE (ASN 87) SUBTILISIN FROM BACILLUS LENTUS |
17.6 |
52.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1iaw |
CRYSTAL STRUCTURE OF NAEI COMPLEXED WITH 17MER DNA |
29.8 |
96.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1iax |
CRYSTAL STRUCTURE OF ACC SYNTHASE COMPLEXED WITH PLP |
29.5 |
88.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1iay |
CRYSTAL STRUCTURE OF ACC SYNTHASE COMPLEXED WITH COFACTOR PLP AND INHIBITOR AVG |
23.0 |
73.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1iaz |
EQUINATOXIN II |
23.8 |
77.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ib0 |
CRYSTAL STRUCTURE OF RAT B5R IN COMPLEX WITH FAD AND NAD |
20.0 |
60.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ib1 |
CRYSTAL STRUCTURE OF THE 14-3-3 ZETA:SEROTONIN N-ACETYLTRANSFERASE COMPLEX |
43.5 |
134.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1ib2 |
CRYSTAL STRUCTURE OF A PUMILIO-HOMOLOGY DOMAIN |
27.3 |
88.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ib4 |
Crystal Structure of Polygalacturonase from Aspergillus Aculeatus at Ph4.5 |
27.1 |
93.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1ib5 |
X-RAY 3D STRUCTURE OF P.LEIOGNATHI CU,ZN SOD MUTANT W83Y |
15.4 |
53.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ib6 |
CRYSTAL STRUCTURE OF R153C E. COLI MALATE DEHYDROGENASE |
34.6 |
107.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ib7 |
SOLUTION STRUCTURE OF F35Y MUTANT OF RAT FERRO CYTOCHROME B5, A CONFORMATION, ENSEMBLE OF 20 STRUCTURES |
12.4 |
42.5 |
SOLUTION NMR |
GOOD
|
| 1ib8 |
SOLUTION STRUCTURE AND FUNCTION OF A CONSERVED PROTEIN SP14.3 ENCODED BY AN ESSENTIAL STREPTOCOCCUS PNEUMONIAE GENE |
22.1 |
71.4 |
SOLUTION NMR |
GOOD
|
| 1ib9 |
SOLUTION STRUCTURE OF MCOTI-II, A MACROCYCLIC TRYPSIN INHIBITOR |
7.7 |
29.9 |
SOLUTION NMR |
GOOD
|
| 1iba |
GLUCOSE PERMEASE (DOMAIN IIB), NMR, 11 STRUCTURES |
12.6 |
40.5 |
SOLUTION NMR |
GOOD
|
| 1ibb |
X-RAY 3D STRUCTURE OF P.LEIOGNATHI CU,ZN SOD MUTANT W83F |
15.4 |
53.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ibc |
CRYSTAL STRUCTURE OF INHIBITED INTERLEUKIN-1BETA CONVERTING ENZYME |
19.8 |
68.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1ibd |
X-RAY 3D STRUCTURE OF P.LEIOGNATHI CU,ZN SOD MUTANT V29A |
15.3 |
52.4 |
X-RAY DIFFRACTION |
GOOD
|